Reverse current pulse method to restore uniform concentration profiles in ion-selective membranes. Part I: Galvanostatic pulse methods with decreased cycle time

Por Zook, Justin M., Lindner, Ernő
Publicado em 2009

Genomes in a bottle: creating standard reference materials for genomic variation - why, what and how?

Por Zook, Justin M, Salit, Marc
Publicado em 2011

Current-polarized ion-selective membranes: The influence of plasticizer and lipophilic background electrolyte on concentration profiles, resistance, and voltage transients

Por Zook, Justin M., Langmaier, Jan, Lindner, Ernő
Publicado em 2009

Interpretation of chronopotentiometric transients of ion-selective membranes with two transition times

Por Zook, Justin M., Bodor, Sándor, Gyurcsányi, Róbert E., Lindner, Ernő
Publicado em 2010

Challenging a bioinformatic tool’s ability to detect microbial contaminants using in silico whole genome sequencing data

Por Olson, Nathan D., Zook, Justin M., Morrow, Jayne B., Lin, Nancy J.
Publicado no PeerJ (2017)

Synthetic Spike-in Standards Improve Run-Specific Systematic Error Analysis for DNA and RNA Sequencing

Por Zook, Justin M., Samarov, Daniel, McDaniel, Jennifer, Sen, Shurjo K., Salit, Marc
Publicado em 2012

PEPR: pipelines for evaluating prokaryotic references

Por Olson, Nathan D., Zook, Justin M., Samarov, Daniel V., Jackson, Scott A., Salit, Marc L.
Publicado no Anal Bioanal Chem (2016)

Tools for annotation and comparison of structural variation

Por Sedlazeck, Fritz J., Dhroso, Andi, Bodian, Dale L., Paschall, Justin, Hermes, Farrah, Zook, Justin M.
Publicado no F1000Res (2017)

Development and Characterization of Reference Materials for Genetic Testing: Focus on Public Partnerships

Por Kalman, Lisa V., Datta, Vivekananda, Williams, Mickey, Zook, Justin M., Salit, Marc L., Han, Jin-Yeong
Publicado no Ann Lab Med (2016)

Medical implications of technical accuracy in genome sequencing

Por Goldfeder, Rachel L., Priest, James R., Zook, Justin M., Grove, Megan E., Waggott, Daryl, Wheeler, Matthew T., Salit, Marc, Ashley, Euan A.
Publicado no Genome Med (2016)

Genome-wide reconstruction of complex structural variants using read clouds

Por Spies, Noah, Weng, Ziming, Bishara, Alex, McDaniel, Jennifer, Catoe, David, Zook, Justin M., Salit, Marc, West, Robert B., Batzoglou, Serafim, Sidow, Arend
Publicado no Nat Methods (2017)

svclassify: a method to establish benchmark structural variant calls

Por Parikh, Hemang, Mohiyuddin, Marghoob, Lam, Hugo Y. K., Iyer, Hariharan, Chen, Desu, Pratt, Mark, Bartha, Gabor, Spies, Noah, Losert, Wolfgang, Zook, Justin M., Salit, Marc
Publicado no BMC Genomics (2016)

Best practices for evaluating single nucleotide variant calling methods for microbial genomics

Por Olson, Nathan D., Lund, Steven P., Colman, Rebecca E., Foster, Jeffrey T., Sahl, Jason W., Schupp, James M., Keim, Paul, Morrow, Jayne B., Salit, Marc L., Zook, Justin M.
Publicado no Front Genet (2015)

International interlaboratory study comparing single organism 16S rRNA gene sequencing data: Beyond consensus sequence comparisons

Por Olson, Nathan D., Lund, Steven P., Zook, Justin M., Rojas-Cornejo, Fabiola, Beck, Brian, Foy, Carole, Huggett, Jim, Whale, Alexandra S., Sui, Zhiwei, Baoutina, Anna, Dobeson, Michael, Partis, Lina, Morrow, Jayne B.
Publicado no Biomol Detect Quantif (2015)

Principles and Recommendations for Standardizing the Use of the Next-Generation Sequencing Variant File in Clinical Settings

Por Lubin, Ira M., Aziz, Nazneen, Babb, Lawrence J., Ballinger, Dennis, Bisht, Himani, Church, Deanna M., Cordes, Shaun, Eilbeck, Karen, Hyland, Fiona, Kalman, Lisa, Landrum, Melissa, Lockhart, Edward R., Maglott, Donna, Marth, Gabor, Pfeifer, John D., Rehm, Heidi L., Roy, Somak, Tezak, Zivana, Truty, Rebecca, Ullman-Cullere, Mollie, Voelkerding, Karl V., Worthey, Elizabeth A., Zaranek, Alexander W., Zook, Justin M.
Publicado no J Mol Diagn (2017)

Assuring the quality of next-generation sequencing in clinical laboratory practice

Por Gargis, Amy S, Kalman, Lisa, Berry, Meredith W, Bick, David P, Dimmock, David P, Hambuch, Tina, Lu, Fei, Lyon, Elaine, Voelkerding, Karl V, Zehnbauer, Barbara A, Agarwala, Richa, Bennett, Sarah F, Chen, Bin, Chin, Ephrem L H, Compton, John G, Das, Soma, Farkas, Daniel H, Ferber, Matthew J, Funke, Birgit H, Furtado, Manohar R, Ganova-Raeva, Lilia M, Geigenmüller, Ute, Gunselman, Sandra J, Hegde, Madhuri R, Johnson, Philip L F, Kasarskis, Andrew, Kulkarni, Shashikant, Lenk, Thomas, Liu, C S Jonathan, Manion, Megan, Manolio, Teri A, Mardis, Elaine R, Merker, Jason D, Rajeevan, Mangalathu S, Reese, Martin G, Rehm, Heidi L, Simen, Birgitte B, Yeakley, Joanne M, Zook, Justin M, Lubin, Ira M
Publicado em 2012

Extensive sequencing of seven human genomes to characterize benchmark reference materials

Por Zook, Justin M., Catoe, David, McDaniel, Jennifer, Vang, Lindsay, Spies, Noah, Sidow, Arend, Weng, Ziming, Liu, Yuling, Mason, Christopher E., Alexander, Noah, Henaff, Elizabeth, McIntyre, Alexa B.R., Chandramohan, Dhruva, Chen, Feng, Jaeger, Erich, Moshrefi, Ali, Pham, Khoa, Stedman, William, Liang, Tiffany, Saghbini, Michael, Dzakula, Zeljko, Hastie, Alex, Cao, Han, Deikus, Gintaras, Schadt, Eric, Sebra, Robert, Bashir, Ali, Truty, Rebecca M., Chang, Christopher C., Gulbahce, Natali, Zhao, Keyan, Ghosh, Srinka, Hyland, Fiona, Fu, Yutao, Chaisson, Mark, Xiao, Chunlin, Trow, Jonathan, Sherry, Stephen T., Zaranek, Alexander W., Ball, Madeleine, Bobe, Jason, Estep, Preston, Church, George M., Marks, Patrick, Kyriazopoulou-Panagiotopoulou, Sofia, Zheng, Grace X.Y., Schnall-Levin, Michael, Ordonez, Heather S., Mudivarti, Patrice A., Giorda, Kristina, Sheng, Ying, Rypdal, Karoline Bjarnesdatter, Salit, Marc
Publicado no Sci Data (2016)